Canonical Allele Identifier: PA891855245
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Tyr109His
CA367402690
NM_033507.3:c.325T>C